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New Ru(ii) complex for dual photochemotherapy: release of cathepsin K inhibitor and 1O2 productionElectronic supplementary information (ESI) available. See DOI: 10.1039/c8dt00876k
A new complex, [Ru(tpy)(dppn)(Cbz-Leu-NHCH 2 CN)] 2+ ( 1 , tpy = 2,2′:6′,2′′-terpyridine, dppn = benzo[ i ]dipyrido[3,2- a :2′,3′- c ]phenazine) was synthesized and its photochemical properties were investigated. This complex undergoes photorelease of the Cbz-Leu-NHCH 2 CN ligand, a known cathepsin...
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creator | Rohrabaugh, Thomas N Collins, Kelsey A Xue, Congcong White, Jessica K Kodanko, Jeremy J Turro, Claudia |
description | A new complex, [Ru(tpy)(dppn)(Cbz-Leu-NHCH
2
CN)]
2+
(
1
, tpy = 2,2′:6′,2′′-terpyridine, dppn = benzo[
i
]dipyrido[3,2-
a
:2′,3′-
c
]phenazine) was synthesized and its photochemical properties were investigated. This complex undergoes photorelease of the Cbz-Leu-NHCH
2
CN ligand, a known cathepsin K inhibitor, with a quantum yield,
Φ
450
, of 0.0012(4) in water (
λ
irr
= 450 nm). In addition,
1
sensitizes the production of singlet oxygen upon visible light irradiation with quantum yield,
Φ
Δ
, of 0.64(3) in CH
3
OH. The photophysical properties of
1
were compared with those of [Ru(tpy)(bpy)(Cbz-Leu-NHCH
2
CN)]
2+
(
2
, bpy = 2,2′-bipyridine), [Ru(tpy)(dppn)(CH
3
CN)]
2+
(
3
), and [Ru(tpy)(bpy)(CH
3
CN)]
2+
(
4
) to evaluate the effect of the release of the Cbz-Leu-NHCH
2
CN inhibitor relative to the CH
3
CN ligand, as well as the role of dppn as the bidentate ligand for
1
O
2
production instead of bpy. Nanosecond transient absorption spectroscopy confirms the formation of the long-lived dppn-centered
3
ππ* state in
1
and
3
with a maximum at ∼540 nm and
τ
∼20 μs in deaerated acetonitrile. Complexes
1
and
3
are able to cause photoinduced damage to DNA (
λ
irr
≥ 395 nm), whereas
2
and
4
do not photocleave DNA under similar experimental conditions. These results suggest that
1
is a promising agent for dual activity, both releasing a drug and producing singlet oxygen, and is poised to exhibit enhanced biological activity in phototochemotherapy upon irradiation with visible light.
A new Ru(
ii
) complex releases a cysteine protease inhibitor and produces cytotoxic
1
O
2
upon irradiation with visible light, making it potentially useful as a dual-action PDT agent. |
doi_str_mv | 10.1039/c8dt00876k |
format | article |
fullrecord | <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c8dt00876k</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c8dt00876k</sourcerecordid><originalsourceid>FETCH-rsc_primary_c8dt00876k3</originalsourceid><addsrcrecordid>eNqFT8tKAzEUDaJgfWzcC9ddu2jNZGpfWztiESxY98Nt5g4TzSQhyaj9Ln_QCKILQVf3cM-Lw9hZxkcZz-eXclZFzmfTyfMe62Xj6XQ4F_l4_xuLySE7CuGJcyH4leix93t6hYeur9QApG2dpjeorYeqQw2usdHKhlobG_LodgvwpAkDga1BYvq6oAzcgTKN2qqYjGgqyNYCnLdVJ6OyptAko7dGSQidSw0tmYh-l0ypqcVPDfSLzWoA-IJK41bTCDZEsFyvFvB72gk7qFEHOv26x-z8pni8vh36IEvnVZvCyx95_j9_8RdfuqrOPwDd_G2t</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>New Ru(ii) complex for dual photochemotherapy: release of cathepsin K inhibitor and 1O2 productionElectronic supplementary information (ESI) available. See DOI: 10.1039/c8dt00876k</title><source>Royal Society of Chemistry</source><creator>Rohrabaugh, Thomas N ; Collins, Kelsey A ; Xue, Congcong ; White, Jessica K ; Kodanko, Jeremy J ; Turro, Claudia</creator><creatorcontrib>Rohrabaugh, Thomas N ; Collins, Kelsey A ; Xue, Congcong ; White, Jessica K ; Kodanko, Jeremy J ; Turro, Claudia</creatorcontrib><description>A new complex, [Ru(tpy)(dppn)(Cbz-Leu-NHCH
2
CN)]
2+
(
1
, tpy = 2,2′:6′,2′′-terpyridine, dppn = benzo[
i
]dipyrido[3,2-
a
:2′,3′-
c
]phenazine) was synthesized and its photochemical properties were investigated. This complex undergoes photorelease of the Cbz-Leu-NHCH
2
CN ligand, a known cathepsin K inhibitor, with a quantum yield,
Φ
450
, of 0.0012(4) in water (
λ
irr
= 450 nm). In addition,
1
sensitizes the production of singlet oxygen upon visible light irradiation with quantum yield,
Φ
Δ
, of 0.64(3) in CH
3
OH. The photophysical properties of
1
were compared with those of [Ru(tpy)(bpy)(Cbz-Leu-NHCH
2
CN)]
2+
(
2
, bpy = 2,2′-bipyridine), [Ru(tpy)(dppn)(CH
3
CN)]
2+
(
3
), and [Ru(tpy)(bpy)(CH
3
CN)]
2+
(
4
) to evaluate the effect of the release of the Cbz-Leu-NHCH
2
CN inhibitor relative to the CH
3
CN ligand, as well as the role of dppn as the bidentate ligand for
1
O
2
production instead of bpy. Nanosecond transient absorption spectroscopy confirms the formation of the long-lived dppn-centered
3
ππ* state in
1
and
3
with a maximum at ∼540 nm and
τ
∼20 μs in deaerated acetonitrile. Complexes
1
and
3
are able to cause photoinduced damage to DNA (
λ
irr
≥ 395 nm), whereas
2
and
4
do not photocleave DNA under similar experimental conditions. These results suggest that
1
is a promising agent for dual activity, both releasing a drug and producing singlet oxygen, and is poised to exhibit enhanced biological activity in phototochemotherapy upon irradiation with visible light.
A new Ru(
ii
) complex releases a cysteine protease inhibitor and produces cytotoxic
1
O
2
upon irradiation with visible light, making it potentially useful as a dual-action PDT agent.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c8dt00876k</identifier><language>eng</language><creationdate>2018-08</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Rohrabaugh, Thomas N</creatorcontrib><creatorcontrib>Collins, Kelsey A</creatorcontrib><creatorcontrib>Xue, Congcong</creatorcontrib><creatorcontrib>White, Jessica K</creatorcontrib><creatorcontrib>Kodanko, Jeremy J</creatorcontrib><creatorcontrib>Turro, Claudia</creatorcontrib><title>New Ru(ii) complex for dual photochemotherapy: release of cathepsin K inhibitor and 1O2 productionElectronic supplementary information (ESI) available. See DOI: 10.1039/c8dt00876k</title><description>A new complex, [Ru(tpy)(dppn)(Cbz-Leu-NHCH
2
CN)]
2+
(
1
, tpy = 2,2′:6′,2′′-terpyridine, dppn = benzo[
i
]dipyrido[3,2-
a
:2′,3′-
c
]phenazine) was synthesized and its photochemical properties were investigated. This complex undergoes photorelease of the Cbz-Leu-NHCH
2
CN ligand, a known cathepsin K inhibitor, with a quantum yield,
Φ
450
, of 0.0012(4) in water (
λ
irr
= 450 nm). In addition,
1
sensitizes the production of singlet oxygen upon visible light irradiation with quantum yield,
Φ
Δ
, of 0.64(3) in CH
3
OH. The photophysical properties of
1
were compared with those of [Ru(tpy)(bpy)(Cbz-Leu-NHCH
2
CN)]
2+
(
2
, bpy = 2,2′-bipyridine), [Ru(tpy)(dppn)(CH
3
CN)]
2+
(
3
), and [Ru(tpy)(bpy)(CH
3
CN)]
2+
(
4
) to evaluate the effect of the release of the Cbz-Leu-NHCH
2
CN inhibitor relative to the CH
3
CN ligand, as well as the role of dppn as the bidentate ligand for
1
O
2
production instead of bpy. Nanosecond transient absorption spectroscopy confirms the formation of the long-lived dppn-centered
3
ππ* state in
1
and
3
with a maximum at ∼540 nm and
τ
∼20 μs in deaerated acetonitrile. Complexes
1
and
3
are able to cause photoinduced damage to DNA (
λ
irr
≥ 395 nm), whereas
2
and
4
do not photocleave DNA under similar experimental conditions. These results suggest that
1
is a promising agent for dual activity, both releasing a drug and producing singlet oxygen, and is poised to exhibit enhanced biological activity in phototochemotherapy upon irradiation with visible light.
A new Ru(
ii
) complex releases a cysteine protease inhibitor and produces cytotoxic
1
O
2
upon irradiation with visible light, making it potentially useful as a dual-action PDT agent.</description><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFT8tKAzEUDaJgfWzcC9ddu2jNZGpfWztiESxY98Nt5g4TzSQhyaj9Ln_QCKILQVf3cM-Lw9hZxkcZz-eXclZFzmfTyfMe62Xj6XQ4F_l4_xuLySE7CuGJcyH4leix93t6hYeur9QApG2dpjeorYeqQw2usdHKhlobG_LodgvwpAkDga1BYvq6oAzcgTKN2qqYjGgqyNYCnLdVJ6OyptAko7dGSQidSw0tmYh-l0ypqcVPDfSLzWoA-IJK41bTCDZEsFyvFvB72gk7qFEHOv26x-z8pni8vh36IEvnVZvCyx95_j9_8RdfuqrOPwDd_G2t</recordid><startdate>20180829</startdate><enddate>20180829</enddate><creator>Rohrabaugh, Thomas N</creator><creator>Collins, Kelsey A</creator><creator>Xue, Congcong</creator><creator>White, Jessica K</creator><creator>Kodanko, Jeremy J</creator><creator>Turro, Claudia</creator><scope/></search><sort><creationdate>20180829</creationdate><title>New Ru(ii) complex for dual photochemotherapy: release of cathepsin K inhibitor and 1O2 productionElectronic supplementary information (ESI) available. See DOI: 10.1039/c8dt00876k</title><author>Rohrabaugh, Thomas N ; Collins, Kelsey A ; Xue, Congcong ; White, Jessica K ; Kodanko, Jeremy J ; Turro, Claudia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c8dt00876k3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rohrabaugh, Thomas N</creatorcontrib><creatorcontrib>Collins, Kelsey A</creatorcontrib><creatorcontrib>Xue, Congcong</creatorcontrib><creatorcontrib>White, Jessica K</creatorcontrib><creatorcontrib>Kodanko, Jeremy J</creatorcontrib><creatorcontrib>Turro, Claudia</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rohrabaugh, Thomas N</au><au>Collins, Kelsey A</au><au>Xue, Congcong</au><au>White, Jessica K</au><au>Kodanko, Jeremy J</au><au>Turro, Claudia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Ru(ii) complex for dual photochemotherapy: release of cathepsin K inhibitor and 1O2 productionElectronic supplementary information (ESI) available. See DOI: 10.1039/c8dt00876k</atitle><date>2018-08-29</date><risdate>2018</risdate><volume>47</volume><issue>34</issue><spage>11851</spage><epage>11858</epage><pages>11851-11858</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>A new complex, [Ru(tpy)(dppn)(Cbz-Leu-NHCH
2
CN)]
2+
(
1
, tpy = 2,2′:6′,2′′-terpyridine, dppn = benzo[
i
]dipyrido[3,2-
a
:2′,3′-
c
]phenazine) was synthesized and its photochemical properties were investigated. This complex undergoes photorelease of the Cbz-Leu-NHCH
2
CN ligand, a known cathepsin K inhibitor, with a quantum yield,
Φ
450
, of 0.0012(4) in water (
λ
irr
= 450 nm). In addition,
1
sensitizes the production of singlet oxygen upon visible light irradiation with quantum yield,
Φ
Δ
, of 0.64(3) in CH
3
OH. The photophysical properties of
1
were compared with those of [Ru(tpy)(bpy)(Cbz-Leu-NHCH
2
CN)]
2+
(
2
, bpy = 2,2′-bipyridine), [Ru(tpy)(dppn)(CH
3
CN)]
2+
(
3
), and [Ru(tpy)(bpy)(CH
3
CN)]
2+
(
4
) to evaluate the effect of the release of the Cbz-Leu-NHCH
2
CN inhibitor relative to the CH
3
CN ligand, as well as the role of dppn as the bidentate ligand for
1
O
2
production instead of bpy. Nanosecond transient absorption spectroscopy confirms the formation of the long-lived dppn-centered
3
ππ* state in
1
and
3
with a maximum at ∼540 nm and
τ
∼20 μs in deaerated acetonitrile. Complexes
1
and
3
are able to cause photoinduced damage to DNA (
λ
irr
≥ 395 nm), whereas
2
and
4
do not photocleave DNA under similar experimental conditions. These results suggest that
1
is a promising agent for dual activity, both releasing a drug and producing singlet oxygen, and is poised to exhibit enhanced biological activity in phototochemotherapy upon irradiation with visible light.
A new Ru(
ii
) complex releases a cysteine protease inhibitor and produces cytotoxic
1
O
2
upon irradiation with visible light, making it potentially useful as a dual-action PDT agent.</abstract><doi>10.1039/c8dt00876k</doi><tpages>8</tpages></addata></record> |
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title | New Ru(ii) complex for dual photochemotherapy: release of cathepsin K inhibitor and 1O2 productionElectronic supplementary information (ESI) available. See DOI: 10.1039/c8dt00876k |
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